FDA Investigator

Gary J Lehr

Latest inspection on record: Amityville, United States, December 2009 · records back to 2008

FDA inspection record · Last updated July 12, 2026

Overview

  • 12 inspections across 10 sites are on record.
  • 43 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2009-12-03.

At a glance

Inspections

12

Sites

10

Observations

43

Career since

Mar 2008

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Hi-Tech Pharmacal, an AKORN Company3 Dec 2009On file
Time-Cap Laboratories, Inc.29 Jun 2009On file
Altaire Pharmaceuticals, Inc.28 Apr 2009On file
Corwood Labs Inc8 Apr 2009View 483 →
Intermax Pharmaceuticals, Inc.3 Feb 2009On file

Sites inspected

Hi-Tech Pharmacal, an AKORN CompanyAmityville, United States1 insp.
Time-Cap Laboratories, Inc.Farmingdale, United States1 insp.
Altaire Pharmaceuticals, Inc.Aquebogue, United States1 insp.
Corwood Labs IncHauppauge, United States1 insp.
Intermax Pharmaceuticals, Inc.Farmingdale, United States1 insp.

Co-investigators

Investigators who share inspections with this person.

Full investigator report

Get the verbatim findings behind Gary J Lehr's 43 observations

Source 483 PDFs, verbatim observations, and how each site responded, so your team knows what they cite before they arrive.

  • New inspections and Form 483s, mapped to the CFR citation
  • Warning letter outcomes, and the citation patterns they repeat
  • Their co-investigators, so no surprises about who shows up on site